GoutFlex Gout Symptom Formula

Drug Facts__________________________________________________________________________________________________________

HPUS active ingredients Purpose †

Equal volumes of each ingredient in 10X, 30X and LM1 potencies.

Ammonium phosphoricum, Belladonna, Colchicum autumnale, Formicum acidum, Fraxinus excelsior, Ledum palustre, Natrum carbonicum, Nux vomica, Urtica urens.

Uses for temporary relief of symptoms in toes, heels, feet, or joints: • discomforts • cramping • tender or itchy joints.

Warnings

If symptoms persist or worsen, seek advice of a physician.
If pregnant or breast-feeding, ask a healthcare professional before use.

Keep out of reach of children.

Directions

Initially, depress pump until primed. Spray one dose directly into mouth. Adults: 4 sprays 2 times per day. (approximately every 12 hours) Use additionally as needed, up to 3 times per day.

Other Information: This product is intended to complement, not replace, standard medical care.

This product has not been clinically tested. Homeopathic provings for each HPUS ingredient are found in various materia medicas referenced in the FDA Compliance Policy Guide.

Manufactured for: Nutra Vista Health, LLC. 3632 Land O Lakes Blvd 106-14 Land O Lakes, FL, 34639 Questions? Call 813.926.7903 www.goutflex.com

Inactive Ingredients:

Citric acid, potassium sorbate, pure water.

Drug Facts

__________________________________________________________________________________________________________

HPUS active ingredients Purpose †

Equal volumes of each ingredient in 10X, 30X and LM1 potencies.

Ammonium phosphoricum...........................inflammation of joints

Belladonna.................................................red and tender joints

Colchicum autumnale......................................sensitivity to touch

Formicum acidum...............................................joint discomfort

Fraxinus excelsior...................................foot-related discomforts

Ledum palustre...................................swelling of joints and toes

Natrum carbonicum...............................................tender joints

Nux vomica..................................................................itching

Urtica urens.....................................................joint discomfort

image description

GOUTFLEX GOUT SYMPTOM FORMULA
ammonium phosphoricum, belladonna, colchicum autumnale, formicum acidum, fraxinus excelsior, ledum palustre, natrum carbonicum, nux vomica, urtica urens liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69760-0001
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (PHOSPHATE ION - UNII:NK08V8K8HR)	AMMONIUM PHOSPHATE, DIBASIC	10 [hp_X] in 59 mL
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H)	ATROPA BELLADONNA	10 [hp_X] in 59 mL
COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (COLCHICUM AUTUMNALE BULB - UNII:993QHL78E6)	COLCHICUM AUTUMNALE BULB	10 [hp_X] in 59 mL
FORMIC ACID (UNII: 0YIW783RG1) (FORMIC ACID - UNII:0YIW783RG1)	FORMIC ACID	10 [hp_X] in 59 mL
FRAXINUS EXCELSIOR BARK (UNII: R6KCX5H8I2) (FRAXINUS EXCELSIOR BARK - UNII:R6KCX5H8I2)	FRAXINUS EXCELSIOR BARK	10 [hp_X] in 59 mL
FRAXINUS EXCELSIOR LEAF (UNII: RC38362Q7M) (FRAXINUS EXCELSIOR LEAF - UNII:RC38362Q7M)	FRAXINUS EXCELSIOR LEAF	10 [hp_X] in 59 mL
LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P)	LEDUM PALUSTRE TWIG	10 [hp_X] in 59 mL
SODIUM CARBONATE (UNII: 45P3261C7T) (CARBONATE ION - UNII:7UJQ5OPE7D)	SODIUM CARBONATE	10 [hp_X] in 59 mL
STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919)	STRYCHNOS NUX-VOMICA SEED	10 [hp_X] in 59 mL
URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9)	URTICA URENS	10 [hp_X] in 59 mL

Ingredient Name	Strength
Inactive Ingredients
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69760-0001-2	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/28/2015

Labeler - Nutra Vista Health LLC. (079775793)

Registrant - Nutra Vista Health LLC. (079775793)